Blackish Discoloration of Articular Cartilage during Total Knee Replacement; a Case Report.

Dhrushith Ettakkepraven Puthanveetil, Vivek Panoor Subhash, Ansari Noohu Kannu, Kevin Kavalakkatt
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Abstract

Introduction: Alkaptonuria is a rare metabolic disorder that follows an autosomal recessive genetic inheritance pattern. It is distinguished by the buildup of homogentisic acid in tissues due to deficient homogentisic acid oxidase enzyme activity. The excess homogentisic acid is expelled through urine, darkening it on oxidation. Moreover, it deposits in connective tissues, imparting a characteristic blue-black pigmentation. This condition is known as Ochronosis or black bone disease. This accumulation over time renders cartilage brittle, potentially leading to ochronotic arthropathy.

Case report: A 46-year-old lady presented with long-standing bilateral knee pain for 8 years with a predominant focus on the right side. Recurrent swelling and pain episodes in the right knee were noted, occurring without significant traumatic events. Despite various conservative treatments attempted to alleviate her knee pain, the patient experienced minimal relief. On examination, the patient demonstrated difficulty in ambulating, with severe tenderness along the joint line and a restricted range of motion. Standing knee X-rays revealed severe tricompartmental osteoarthritis and a correctable valgus deformity of 5. She underwent total knee replacement. A provisional diagnosis of ochronosis was made intraoperatively, later confirmed on histopathological examination of the tissue, and the patient was evaluated retrospectively.

Conclusion: Ochronotic arthropathies are rare conditions- characterized by articular cartilage damage. They are typically diagnosed post-surgery, often when surgeons observe the dark coloration of cartilage. However, joint replacement surgery can safely and effectively manage these conditions, leading to favorable outcomes, including improved functionality, pain alleviation, and heightened patient satisfaction.

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简介碱蛋白尿是一种罕见的代谢性疾病,为常染色体隐性遗传。这种疾病的特征是,由于高戊酸氧化酶活性不足,组织中会积聚高戊酸。过量的高戊二酸会通过尿液排出,并在氧化过程中使尿液变黑。此外,它还会沉积在结缔组织中,形成特有的蓝黑色色素沉着。这种情况被称为 Ochronosis 或黑色骨病。随着时间的推移,这种积累会使软骨变脆,可能导致chronotic 关节病:一位 46 岁的女士因双侧膝关节疼痛长达 8 年之久,疼痛主要集中在右侧。右膝盖反复肿胀和疼痛,且无明显外伤。尽管患者尝试了各种保守疗法来缓解膝关节疼痛,但缓解效果甚微。经检查,患者行走不便,关节沿线有严重压痛,活动范围受限。站立时的膝关节X光片显示,患者患有严重的三室骨关节炎,膝关节外翻畸形达到5度。她接受了全膝关节置换术。术中临时诊断为chronosis,后经组织病理学检查确诊,并对患者进行了回顾性评估:chronotic关节病是一种罕见的疾病,以关节软骨损伤为特征。它们通常是在手术后被诊断出来的,通常是在外科医生观察到软骨颜色变深的时候。然而,关节置换手术可以安全有效地控制这些病症,从而获得良好的治疗效果,包括改善功能、减轻疼痛和提高患者满意度。
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